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One-pot two-step microwave-assisted reaction in constructing 4,5-disubstituted pyrazolopyrimidines

Academic Article
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Overview

related to degree

  • Wu, Tom, Ph.D. in Chemistry, Scripps Research 2000 - 2003
  • Ding, Sheng, Ph.D. in Chemistry, Scripps Research 1999 - 2003

authors

  • Wu, Tom
  • Schultz, Peter
  • Ding, Sheng

publication date

  • October 2003

journal

  • Organic Letters  Journal

abstract

  • [reaction: see text] A microwave-assisted reaction was developed to facilitate the construction of 4,5-disubstituted pyrazolopyrimidines. This one-pot two-step process involves a sequential S(N)Ar displacement of the C4 chloro substituent with various anilines and amines, followed by a Suzuki coupling reaction with different boronic acids. Using microwave irradiation leads to high product conversion, low side product formation, and shorter reactions.
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Identity

International Standard Serial Number (ISSN)

  • 1523-7060

Digital Object Identifier (DOI)

  • 10.1021/ol035226w

PubMed ID

  • 14507179
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Additional Document Info

start page

  • 3587

end page

  • 3590

volume

  • 5

issue

  • 20

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